CN101624350A - Crystallization method of 5-aminolevulinic propionic hydrochloride - Google Patents
Crystallization method of 5-aminolevulinic propionic hydrochloride Download PDFInfo
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- CN101624350A CN101624350A CN200910100980A CN200910100980A CN101624350A CN 101624350 A CN101624350 A CN 101624350A CN 200910100980 A CN200910100980 A CN 200910100980A CN 200910100980 A CN200910100980 A CN 200910100980A CN 101624350 A CN101624350 A CN 101624350A
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- acid hydrochloride
- aminolevulinic acid
- aminolevulinic
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Abstract
The invention relates to a crystallization method of 5-aminolevulinic propionic hydrochloride. The crystallization method comprises the following steps: gradually cooling an aqueous solution of doped 5-aminolevulinic propionic hydrochloride with the mass concentration of 300-600 g/L at an initial temperature of 60-70 DEG C under a stirring condition with a stirring rotation speed of 50-300 rpm while controlling a cooling rate of a crystallization process to be 5-15 DEG C/hour; stopping stirring when a great amount of crystal nucleus are generated; growing crystals at a constant temperature for 0.5-2 hours, wherein a final temperature for crystallization is from 10 DEG C below zero to 15 DEG C; filtering, separating, washing and drying the obtained crystals to obtain needle crystals of the 5-aminolevulinic propionic hydrochloride. The obtained 5-aminolevulinic propionic hydrochloride has higher crystallization purity and favorable stability, the method has shorter crystallization time and environment-friendly crystallization process, thereby having low cost and high efficiency.
Description
Technical field
The present invention relates to a kind of crystallization method of 5-aminolevulinic acid hydrochloride.
Background technology
(5-aminolevulinic acid is the common precursor of Pyrrolidine compounds in the organism ALA) to the 5-amino-laevulic acid, can be used for hemachrome enzyme, porphyrin and vitamins B in the microbial fermentation field
12Preparation Deng compound.ALA can be used as the high and environment amenable photo-activation pesticide of selectivity on agricultural.At medical field, the 5-amino-laevulic acid is having great using value as photodynamics medicine of new generation aspect the diagnosis of diseases such as brain tumor, skin carcinoma and the treatment.
The production method of 5-amino-laevulic acid can be divided into chemical synthesis and microbe fermentation method.Chemosynthesis ALA has number of ways, can be the synthetic ALA of raw material with urobenzoic acid, succsinic acid, tetrahydrofurfuryl amine and levulinic acid etc. respectively, but the complex steps of chemosynthesis ALA, and productive rate is low and by product is many.For microbe fermentation method, producing the 5-amino-laevulic acid by the structure genetic engineering bacterium is a kind of cheapness and effective means.Disclose among the CN101063105 and a kind ofly come the method for fermentative production ALA by genetic engineering bacterium Rosetta (DE3)-pET28a-A.R.hemA, wherein the output of ALA can reach 6.5g/L.
The technology of condensing crystal after the general employing of the separation of the ALA purification ion-exchange in the fermented liquid.A kind of 5-aminolevulinic acid hydrochloride crystalline method is disclosed among the CN1942430, it is for to join poor solvent in the 5-aminolevulinic acid hydrochloride aqueous solution of high density, thereby make 5-aminolevulinic acid hydrochloride crystal separate out, used poor solvent can be alcohol, ether, ester, nitrile etc., methyl acetate wherein, gamma-butyrolactone, acetone or acetonitrile are preferred solvent.Disclosed method also is to separate out 5-aminolevulinic acid hydrochloride crystal by sneak into poor solvent in the aqueous solution among the CN101268036, and wherein ethanol, acetone, Virahol are preferred solvent.But above-mentioned crystallization method all need use a large amount of organic solvents, and production cost is higher, and environment is produced bigger pollution.
Summary of the invention
The object of the present invention is to provide that a kind of crystallization purity is higher, stability better, cost is low and the environment amenable 5-aminolevulinic acid hydrochloride of process crystalline method.
The crystallization method of 5-aminolevulinic acid hydrochloride of the present invention may further comprise the steps:
With initial temperature is that 60～70 ℃, mass concentration are that the aqueous solution of 5-aminolevulinic acid hydrochloride of 300～600g/L is under agitation condition, with the rate of temperature fall of 5～15 ℃/hr decrease temperature crystalline gradually, mixing speed is 50～300rpm, when temperature is reduced to-10～15 ℃, there is nucleus to generate, stop to stir, behind-10～15 ℃ of following constant temperature growing the grain 0.5～2h, suction filtration separates, with acetone or ether washing crystal, vacuum-drying 2～6h under the normal temperature obtains the needle crystal of 5-aminolevulinic acid hydrochloride.
Can contain other impurity in the above-mentioned 5-aminolevulinic acid hydrochloride aqueous solution, said impurity is one or more in chlorion, sodium ion, ammonium ion, amino acid, organic acid and the pigment.The 5-aminolevulinic acid hydrochloride aqueous solution also can be the thick solution that process degerming or ion-exchange initial gross separation obtain.
In order to improve crystallization yields, the mother liquor activated carbon decolorizing after can taking suction filtration separated carries out secondary crystal at reduction vaporization under 60～70 ℃ of water-baths, after concentrated.
Crystallization method provided by the invention is that the aqueous solution of the 5-aminolevulinic acid hydrochloride of high density is come crystallization by cooling.Adopt aforesaid method, the 5-aminolevulinic acid hydrochloride crystalline purity that obtains can reach more than 99.5%, and the secondary crystallization total recovery reaches 78.7%.The principal feature of this method is that 5-aminolevulinic acid hydrochloride crystal directly separates out from the aqueous solution.Compared with prior art, the present invention has avoided the use of a large amount of organic solvent, has reduced and has realized the step that crystallization needs, and has saved production time and cost, and production process is environmentally friendly.
Embodiment
Further specify this invention below in conjunction with embodiment
Embodiment 1
The source of the aqueous solution of 5-aminolevulinic acid hydrochloride: the fermented liquid 19.0L that has removed the 5-amino-laevulic acid of thalline, wherein ALA concentration is 3.2g/L, after the ion-exchange separation, elutriant is handled with 100ml 5M hcl acidifying, obtains the thick aqueous solution of the 5-aminolevulinic acid hydrochloride (ALAHCl) of 1320ml, and wherein ALAHCl concentration is 28.8g/L, activated carbon decolorizing with 1%, suction filtration behind the stirring 20min, filter cake washs with small amount of deionized water, obtains the filtrate of 1325ml.The destainer rotary evaporation that under 65 ℃ of water-baths, reduces pressure, obtain the aqueous solution of the 5-aminolevulinic acid hydrochloride of 98ml at last, wherein ALAHCl concentration is 380.6g/L, contains impurity such as chlorion, sodium ion, ammonium ion, amino acid, organic acid and pigment in the solution.
The aqueous solution of above-mentioned 5-aminolevulinic acid hydrochloride is stirred under the 150rpm rotating speed, with the rate of temperature fall of 10 ℃/hr decrease temperature crystalline gradually, stop to stir when having nucleus to generate, respectively at 15 ℃, constant temperature growing the grain 1h under 10 ℃, 5 ℃, 0 ℃ ,-5 ℃ ,-10 ℃ the temperature, get the upper strata saturated solution, measure the saturation solubility under the variant temperature.The result is as shown in table 1, and by table as seen, along with the reduction of Tc, the crystallization yields of ALAHCl raises gradually.
The saturation solubility of ALAHCl under table 1 differing temps
| Temperature (℃) | ??15 | ??10 | ??5 | ??0 | ??-5 | ??-10 |
| Saturation solubility (g/100ml H 2O) | ??326.1 | ??280.7 | ??256.1 | ??206.1 | ??178.0 | ??153.4 |
Behind-10 ℃ of following constant temperature growing the grain 2h, suction filtration gets the crystal of 5-aminolevulinic acid hydrochloride, and the washing with acetone crystal of usefulness 30ml once.Obtain ALAHCl crystal 19.4g behind the vacuum-drying 5h.Degree of purity of production is 99.7%, and yield is 51.1%.
Embodiment 2
The concentrated solution of 5-aminolevulinic acid hydrochloride behind primary crystallization, remaining mother liquor 250ml, wherein ALAHCl concentration is 270.4g/L.Activated carbon decolorizing with 2%, stir suction filtration behind the 20min, filter cake washs with small amount of deionized water, the filtrate that the obtains rotary evaporation that reduces pressure under 65 ℃ of water-baths, obtain the concentrated solution of the 5-aminolevulinic acid hydrochloride of 113ml at last, wherein ALAHCl concentration is 587.5g/L.Under the rotating speed of 100rpm, stir,, have nucleus to generate with the rate of temperature fall of 10 ℃/hr decrease temperature crystalline gradually, stop to stir, behind the constant temperature growing the grain 2h, suction filtration got 5-aminolevulinic acid hydrochloride crystal when temperature dropped to-10 ℃, use the 40ml washing with acetone, get ALAHCl crystal 3 9.6g after the drying.Crystalline purity is 99.5%, and the yield of secondary crystal is 58.6%.
Embodiment 3
The source of the aqueous solution of 5-aminolevulinic acid hydrochloride: the fermented liquid 18.1L that has removed the 5-amino-laevulic acid of thalline, wherein ALA concentration is 4.2g/L, after the ion-exchange separation, elutriant 5M hydrochloric acid 120ml acidification, obtain the thick aqueous solution of the 5-aminolevulinic acid hydrochloride of 1760ml, wherein ALAHCl concentration is 34.5g/L, activated carbon decolorizing with 1.5%, suction filtration behind the stirring 30min, filter cake washs with small amount of deionized water, the filtrate that the obtains rotary evaporation that reduces pressure under 65 ℃ of water-baths obtains the concentrated solution of 118ml 5-aminolevulinic acid hydrochloride at last.Wherein the concentration of ALAHCl is 505.9g/L, contains impurity such as chlorion, sodium ion, ammonium ion, amino acid, organic acid and pigment in the solution.
Above-mentioned ALAHCl concentrated solution is stirred under the 150rpm rotating speed,, stop to stir when having nucleus to generate, at 0 ℃ of following constant temperature growing the grain 30min with the rate of temperature fall of 15 ℃/hr decrease temperature crystalline gradually.Suction filtration gets 5-aminolevulinic acid hydrochloride crystal, and the washing with acetone of usefulness 30ml once.Obtain ALAHCl crystal 3 2.0g behind the vacuum-drying 6h.Crystalline mother solution is carried out secondary crystal with the method for embodiment 2, and the volume of mother liquor is 102ml, and the concentration of ALAHCl is 208.7g/L.Obtain the concentrated solution 39ml of 5-aminolevulinic acid hydrochloride behind decolouring, rotary evaporation, wherein ALAHCl concentration is 520.0g/L.Behind the constant temperature growing the grain 2h, suction filtration obtains 5-aminolevulinic acid hydrochloride crystal once more, uses the 20ml washing with acetone in the time of-10 ℃, gets ALAHCl crystal 15.8g after the drying.Crystalline purity is 99.5%, and two-stage crystalline total recovery is 80.1%.
Claims (4)
1. the crystallization method of a 5-aminolevulinic acid hydrochloride is characterized in that may further comprise the steps:
With initial temperature is that 60～70 ℃, mass concentration are that the aqueous solution of 5-aminolevulinic acid hydrochloride of 300～600g/L is under agitation condition, with the rate of temperature fall of 5～15 ℃/hr decrease temperature crystalline gradually, mixing speed is 50～300rpm, when temperature is reduced to-10～15 ℃, there is nucleus to generate, stop to stir, behind-10～15 ℃ of following constant temperature growing the grain 0.5～2h, suction filtration separates, with acetone or ether washing crystal, vacuum-drying 2～6h under the normal temperature obtains the needle crystal of 5-aminolevulinic acid hydrochloride.
2. the crystallization method of 5-aminolevulinic acid hydrochloride according to claim 1, it is characterized in that containing impurity in the 5-aminolevulinic acid hydrochloride aqueous solution, said impurity is one or more in chlorion, sodium ion, ammonium ion, amino acid, organic acid and the pigment.
3. the crystallization method of 5-aminolevulinic acid hydrochloride according to claim 1 is characterized in that the 5-aminolevulinic acid hydrochloride aqueous solution is the thick solution that fermented liquid process degerming or ion-exchange initial gross separation obtain.
4. the crystallization method of 5-aminolevulinic acid hydrochloride according to claim 1 is characterized in that the mother liquor activated carbon decolorizing after suction filtration separates, and can carry out secondary crystal at reduction vaporization under 60～70 ℃ of water-baths, after concentrated.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103265444A (en) * | 2013-04-24 | 2013-08-28 | 浙江大学 | Crystallization method of 5-aminolevulinic acid phosphate |
| CN108707083A (en) * | 2018-07-02 | 2018-10-26 | 无锡晶海氨基酸股份有限公司 | A method of isolating and purifying branched-chain amino acid from zymotic fluid |
| CN111838421A (en) * | 2020-07-27 | 2020-10-30 | 中国科学院天津工业生物技术研究所 | Method for preparing 5-aminolevulinic acid from fermentation liquor and application thereof |
| CN113912508A (en) * | 2021-08-31 | 2022-01-11 | 新泰市佳禾生物科技有限公司 | Method for separating and purifying 5-aminolevulinic acid from fermentation liquor |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4977349B2 (en) * | 2005-09-21 | 2012-07-18 | コスモ石油株式会社 | Process for producing 5-aminolevulinic acid hydrochloride |
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2009
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103265444A (en) * | 2013-04-24 | 2013-08-28 | 浙江大学 | Crystallization method of 5-aminolevulinic acid phosphate |
| CN108707083A (en) * | 2018-07-02 | 2018-10-26 | 无锡晶海氨基酸股份有限公司 | A method of isolating and purifying branched-chain amino acid from zymotic fluid |
| CN108707083B (en) * | 2018-07-02 | 2021-01-29 | 无锡晶海氨基酸股份有限公司 | Method for separating and purifying branched chain amino acid from fermentation liquor |
| CN111838421A (en) * | 2020-07-27 | 2020-10-30 | 中国科学院天津工业生物技术研究所 | Method for preparing 5-aminolevulinic acid from fermentation liquor and application thereof |
| CN111838421B (en) * | 2020-07-27 | 2023-04-21 | 中国科学院天津工业生物技术研究所 | Method for preparing 5-aminolevulinic acid from fermentation broth and application thereof |
| CN113912508A (en) * | 2021-08-31 | 2022-01-11 | 新泰市佳禾生物科技有限公司 | Method for separating and purifying 5-aminolevulinic acid from fermentation liquor |
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